Bifid nose

Symptom Information:

Symptom ID: HPO:0011803
Synonyms:
Congenital cleft nose (disorder) [Orphanet:8210]
Bifid nose [Orphanet:8210]
Bifid nose [OMIM:Bifid nose]
Bifid tip/cleft nose/supernumerary nose [Orphanet:8210]
Quality:
Cross references:
Orphanet:8210 "Bifid tip/cleft nose/supernumerary nose" [Orphanet:8210]
OMIM: "Bifid nose" [OMIM:Bifid nose]
UMLS:C0221363 "Bifid nose" [Orphanet:8210]
Is a (Direct Parents):
Orphanet Abnormality of the nose
Orphanet Bifid nasal tip
HPO         Midline defect of the nose
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the nose(HPO:0000366)
                   Abnormal nasal morphology(HPO:0005105)
                      Midline defect of the nose(HPO:0004122)
                         Bifid nose(HPO:0011803)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Acromelic frontonasal dysplasia (Orphanet:1827)
BIFID NOSE, AUTOSOMAL DOMINANT (OMIM:109740)
BIFID NOSE, AUTOSOMAL RECESSIVE (OMIM:210400)
BNAR syndrome (Orphanet:217266)
Bifid nose (Orphanet:2695)
FRONTOFACIONASAL DYSPLASIA (OMIM:229400)
Fronto-facio-nasal dysostosis (Orphanet:1791)
HYDROLETHALUS SYNDROME 1 (OMIM:236680)
Hydrolethalus (Orphanet:2189)
Hypertelorism-microtia-facial clefting syndrome (Orphanet:2213)
Neurofaciodigitorenal syndrome (Orphanet:2673)
Trigonocephaly - bifid nose - acral anomalies (Orphanet:3368)